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  2. Phenol oxidation with hypervalent iodine reagents - Wikipedia

    en.wikipedia.org/wiki/Phenol_oxidation_with...

    Bis(phenol) substrates undergo oxidative coupling under these conditions. Iodonium ylides are relatively stable, versatile compounds that undergo substitution and cycloaddition reactions. They are represented using two resonance forms, one zwitterionic (the "betaine" form) and the other neutral (the "ylide" form).

  3. Folin–Ciocalteu reagent - Wikipedia

    en.wikipedia.org/wiki/Folin–Ciocalteu_reagent

    The Folin–Ciocâlteu reagent (FCR) or Folin's phenol reagent or Folin–Denis reagent, is a mixture of phosphomolybdate and phosphotungstate used for the colorimetric in vitro assay of phenolic and polyphenolic antioxidants, also called the gallic acid equivalence method (GAE). [1] It is named after Otto Folin, Vintilă Ciocâlteu, and Willey ...

  4. Phenol - Wikipedia

    en.wikipedia.org/wiki/Phenol

    Phenol is a measurable component in the aroma and taste of the distinctive Islay scotch whisky, [56] generally ~30 ppm, but it can be over 160ppm in the malted barley used to produce whisky. [57] This amount is different from and presumably higher than the amount in the distillate.

  5. Oxidative coupling of phenols - Wikipedia

    en.wikipedia.org/wiki/Oxidative_coupling_of_phenols

    Vanadium tetrachloride is known to effect one-electron oxidations, which is invoked in this conversion. [2] Oxidative coupling of phenol by VCl 4. Coproducts including vanadium(III) and hydrogen chloride are not shown. Oxidative phenol couplings can occur through either inner sphere or outer sphere processes. In inner sphere processes, the ...

  6. Phenol coefficient - Wikipedia

    en.wikipedia.org/wiki/Phenol_coefficient

    To calculate phenol coefficient, the concentration of phenol at which the compound kills the test organism in 10 minutes, but not in 5 minutes, is divided by the concentration of the test compound that kills the organism under the same conditions (or, probably more common, dividing the dilution factor at which the tested substance shows ...

  7. Dow process (phenol) - Wikipedia

    en.wikipedia.org/wiki/Dow_process_(phenol)

    When 1-[14 C]-1-chlorobenzene was subjected to aqueous NaOH at 395 °C, ipso substitution product 1-[14 C]-phenol was formed in 54% yield, while cine substitution product 2-[14 C]-phenol was formed in 43% yield, indicating that an elimination-addition (benzyne) mechanism is predominant, with perhaps a small amount of product from addition ...

  8. Fenton's reagent - Wikipedia

    en.wikipedia.org/wiki/Fenton's_reagent

    The free radicals generated by this process engage in secondary reactions. For example, the hydroxyl is a powerful, non-selective oxidant. [6] Oxidation of an organic compound by Fenton's reagent is rapid and exothermic and results in the oxidation of contaminants to primarily carbon dioxide and water.

  9. Naturally occurring phenols - Wikipedia

    en.wikipedia.org/wiki/Naturally_occurring_phenols

    In female elephants, the two compounds 3-ethyl phenol and 2-ethyl 4,5 dimethylphenol have been detected in urine samples. [70] Temporal glands secretion examination showed the presence of phenol, m-cresol and p-cresol (4-methyl phenol) during musth in male elephants. [71] [72] [73] p-Cresol and o-cresol are also components of the human sweat.